Canonical Allele Identifier: CA2725780

Gene: HTR3C

Linked Data

• dbSNP Id: rs760756384
• ExAC: 3:183778037 T / TA
• gnomAD v2: 3-183778037-T-TA
• gnomAD v4: 3-184060249-T-TA
• MyVariant Identifiers: chr3:g.183778037_183778038insA (hg19) ; chr3:g.184060249_184060250insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184060249_184060250insA , CM000665.2:g.184060249_184060250insA	GRCh38
NC_000003.11:g.183778037_183778038insA , CM000665.1:g.183778037_183778038insA	GRCh37
NC_000003.10:g.185260731_185260732insA	NCBI36
NG_012749.1:g.12203_12204insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318351.2:c.1241_1242insA MANE Select	ENSP00000322617.1:p.Trp415ValfsTer?
ENST00000318351.1:c.1241_1242insA	ENSP00000322617.1:p.Trp415ValfsTer?
NM_130770.2:c.1241_1242insA	NP_570126.2:p.Trp415ValfsTer?
NM_130770.3:c.1241_1242insA MANE Select	NP_570126.2:p.Trp415ValfsTer?